O. DEMİRHAN Et Al. , "Novel striking mismutations on GNAS1 FGF23 and FGF3 genes in CKD with secondary hyperparathroidism and Sağlıker syndrome is a combination compulsion of bone displasias hereditary osteodystrophies and CKD," 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress , London, Canada, 2015
DEMİRHAN, O. Et Al. 2015. Novel striking mismutations on GNAS1 FGF23 and FGF3 genes in CKD with secondary hyperparathroidism and Sağlıker syndrome is a combination compulsion of bone displasias hereditary osteodystrophies and CKD. 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress , (London, Canada).
DEMİRHAN, O., Sağlıker, Y., Akbal, E., Ergun, S., BAYRAKTAR, R., Sağlıker, H. S., ... DOĞAN, E.(2015). Novel striking mismutations on GNAS1 FGF23 and FGF3 genes in CKD with secondary hyperparathroidism and Sağlıker syndrome is a combination compulsion of bone displasias hereditary osteodystrophies and CKD . 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress, London, Canada
DEMİRHAN, OSMAN Et Al. "Novel striking mismutations on GNAS1 FGF23 and FGF3 genes in CKD with secondary hyperparathroidism and Sağlıker syndrome is a combination compulsion of bone displasias hereditary osteodystrophies and CKD," 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress, London, Canada, 2015
DEMİRHAN, OSMAN Et Al. "Novel striking mismutations on GNAS1 FGF23 and FGF3 genes in CKD with secondary hyperparathroidism and Sağlıker syndrome is a combination compulsion of bone displasias hereditary osteodystrophies and CKD." 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress , London, Canada, 2015
DEMİRHAN, O. Et Al. (2015) . "Novel striking mismutations on GNAS1 FGF23 and FGF3 genes in CKD with secondary hyperparathroidism and Sağlıker syndrome is a combination compulsion of bone displasias hereditary osteodystrophies and CKD." 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress , London, Canada.
@conferencepaper{conferencepaper, author={OSMAN DEMİRHAN Et Al. }, title={Novel striking mismutations on GNAS1 FGF23 and FGF3 genes in CKD with secondary hyperparathroidism and Sağlıker syndrome is a combination compulsion of bone displasias hereditary osteodystrophies and CKD}, congress name={52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress}, city={London}, country={Canada}, year={2015}}